[go: up one dir, main page]

US2461551A - Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal - Google Patents

Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal Download PDF

Info

Publication number
US2461551A
US2461551A US640676A US64067646A US2461551A US 2461551 A US2461551 A US 2461551A US 640676 A US640676 A US 640676A US 64067646 A US64067646 A US 64067646A US 2461551 A US2461551 A US 2461551A
Authority
US
United States
Prior art keywords
styrene
coal
butadiene
resin
copolymer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US640676A
Inventor
Ernest D Lee
Loy S Engle
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Interchemical Corp
Original Assignee
Interchemical Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Interchemical Corp filed Critical Interchemical Corp
Priority to US640676A priority Critical patent/US2461551A/en
Application granted granted Critical
Publication of US2461551A publication Critical patent/US2461551A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L9/00Compositions of homopolymers or copolymers of conjugated diene hydrocarbons
    • C08L9/06Copolymers with styrene
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L57/00Compositions of unspecified polymers obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • C08L57/02Copolymers of mineral oil hydrocarbons

Definitions

  • butadiene-styrene rubbery copolymers such as GR-S, Buna S, and the like have gone into extensive use during the past few years, the processing of this type of synthetic rubber presents various difiiculties which render the working thereof prolonged and expensive.
  • butadiene-styrene rubbery copolymers of this type exhibit a decided lack of tack or cohesive bonding, which weakness leads to difiiculty in the handling of such copolymers on conventional rubber-working machinery, especially the customary roll mill.
  • This difficulty in handling evidences itself principally in poor following of the rolls of a roll mill and in poor acceptance or wetting of reinforcing fillers and pigments by such rubbery copolymers.
  • butadiene-styrene rubbery copolymers can be materially improved by incorporating therewith a small amount of a Utah-type coal resin.
  • the presence of the coal resin has been found to reduce the time and the cost of milling a butadiene-styrene copolymer and of incorporating compoundin ingredients therewith.
  • the addition of the coal resin serves to increase the tack of butadiene-styrene copolymers containing from about 20% to about 30% styrene to such an extent that the proces'sability thereof is brought substantially to a par with that of natural rubber.
  • Such a butadiene-styrene rubbery copolymer containing a Utah-type coal resin not only follows rolls properly but also readily accepts the necessary amounts of pigments, fillers, and the like customarily added to rubbery materials during the processing thereof. Moreover, the presence of the Utah-type coal resin does not adversely aiiect the curing of the milled butadiene-styrene rubbery compound, and the cured compounded copolymer exhibits good tensile strength, ultimate elongat on, and hardness.
  • the coal resin which we incorporate with butadiene-styrene copolymers is obtained from resinbearing coals such as those found in extensive deposits in Utah. These coals, particularly those obtained from the Utah deposits, contain substantial percentages (up to 5% and more) of such resinous material, which maybe separated and recovered therefrom in various manners.
  • the resin is preferably employed in a coal-free condition. It can advantageously be recovered from the coal by the following two-stage procedure:
  • the resin is first separated from the bulk of the coal by aqueous flotation as described, for example, in Green, 1,773,997.
  • the resulting resin concentrate which still contains an appreciable proportion of coal (up to 15 to 20%) admixed therewith, is then dissolved in a solvent composed essentially of saturated hydrocarbons having 6 or less carbon atoms in accordance with the disclosure of the copending Lee application, Serial No. 515,804, filed December 27, 1943, now abandoned.
  • the insoluble coal is separated from the resultin resin solution by filtration, and the resin itself is then recovered in a substantially coal-free'condition by vaporization of the solvent from the solution. If a light-colored resin product is desired, the resin solution may be filtered through a bed of activated clay or the like.
  • a typical Utah-type coal resin, recovered in this manner, is soluble in ethers, petroleum and coal-tar hydrocarbons, and vegetable oils, partially soluble in esters and ketones, and insoluble in the lower alcohols.
  • the following physical and chemical characteristics are typical of a representative Utah-type coal resin which has been recovered by extraction with hexane:
  • the coal resin is advantageously compounded with a butadiene-styrene rubbery copolymer, 'especially a copolymer containing from about 20% to about 30% styrene, in an amount ranging from about. 5 to about 25% based on the weightof the copolymer. Within this range of proportions occurs the most significant increase in processibility of the rubbery copolymer with the pro- 3 duction of a cured product having the most desirable characteristics. Less than 5% of the coal resin may be used, but in such case the increase in processibility of the copolymer may not be sufficient to permit the ready incorporation therewith of the desired amounts of pigments and fillers. More than 25% of the coal resin may also be employed.
  • Suilicient coal resin should, of course, be incorporated with the butadiene-styrene copolymer to improve its processing characteristics and to enable it to be broken down on milling to the extent necessary for the desired purpose.
  • the resin may be incorporated with the copolymer either before the copolymer is passed through a roll mill or other rubber handling equipment or during the milling of the copolymer.
  • GH rubber a copolymer of about 75% butadiene and 25% styrene compounded with a coal-free Utah-type coal resin:
  • Example 1 A GR-S-containing tire-tread stock was prepared from the following materials:
  • the presence of the coal resin rendered the milling of the GR-S copolymer and the incorporation of the other ingredients therewith much more easy.
  • the milled copolymer compound possessed an increased dry tack and exhibited an excellent tack when it was washed with gasoline.
  • Example 2 The following formulation illustrates a (33-8 copolymer compound having a very high degree of tackiness.
  • the compoundedGR-S was readily millable.
  • a composition comprising a rubbery copolymer of butadiene and styrene and 5-25% on the weight of the copolymer of a resin consisting essentially of carbon and hydrogen, having an average molecular weight on the order of 1000 and a refractive index of 1.544 and occurring in Utah resin-bearing coals.
  • composition as claimed in claim 1 in which the rubbery copolymer of butadiene and styrene contains from about 20% to about 30% styrene.
  • composition as claimed in claim 1 in which the rubbery copolymer of butadiene and styrene contains approximately butadiene and 25% styrene.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
  • Processes Of Treating Macromolecular Substances (AREA)

Description

Patented Feb. 15, 1949 COMPOSITION COMPRISING A RUBBERY CO- POLYMER OF BUTADIENE AND STYRENE AND A RESIN OCCURRING IN UTAH RESDI- BEARING COAL Ernest D. Lee, Teaneck, and Loy S. Engle, Harrington Park, N. J assignors to Interchemical Corporation, New York, N. Y., a corporation of Ohio No Drawing. Application January 11, 1946,
Serial No. 640,676
6 Claims. (01. 260- 27) diene-styrene rubbery copolymers and is particularly directed to the improvement of the processing characteristics thereof'whereby such copolymers can be more readily handled by the customary rubber-processing equipment. More especially, the present invention is concerned with the improvement of the tackiness of a butadiene-styrene rubbery copolymer containing from about to about 30% styrene.
Although butadiene-styrene rubbery copolymers such as GR-S, Buna S, and the like have gone into extensive use during the past few years, the processing of this type of synthetic rubber presents various difiiculties which render the working thereof prolonged and expensive. In particular, butadiene-styrene rubbery copolymers of this type exhibit a decided lack of tack or cohesive bonding, which weakness leads to difiiculty in the handling of such copolymers on conventional rubber-working machinery, especially the customary roll mill. This difficulty in handling evidences itself principally in poor following of the rolls of a roll mill and in poor acceptance or wetting of reinforcing fillers and pigments by such rubbery copolymers.
We have now found that the processing characteristics of butadiene-styrene rubbery copolymers can be materially improved by incorporating therewith a small amount of a Utah-type coal resin. The presence of the coal resin has been found to reduce the time and the cost of milling a butadiene-styrene copolymer and of incorporating compoundin ingredients therewith. In particular, the addition of the coal resin serves to increase the tack of butadiene-styrene copolymers containing from about 20% to about 30% styrene to such an extent that the proces'sability thereof is brought substantially to a par with that of natural rubber. Such a butadiene-styrene rubbery copolymer containing a Utah-type coal resin not only follows rolls properly but also readily accepts the necessary amounts of pigments, fillers, and the like customarily added to rubbery materials during the processing thereof. Moreover, the presence of the Utah-type coal resin does not adversely aiiect the curing of the milled butadiene-styrene rubbery compound, and the cured compounded copolymer exhibits good tensile strength, ultimate elongat on, and hardness. The
addition of the coal resin also effects a decided reduction in the nerve of the copolymer,
The coal resin which we incorporate with butadiene-styrene copolymers is obtained from resinbearing coals such as those found in extensive deposits in Utah. These coals, particularly those obtained from the Utah deposits, contain substantial percentages (up to 5% and more) of such resinous material, which maybe separated and recovered therefrom in various manners. In accordance with the present invention, the resin is preferably employed in a coal-free condition. It can advantageously be recovered from the coal by the following two-stage procedure:
The resin is first separated from the bulk of the coal by aqueous flotation as described, for example, in Green, 1,773,997. The resulting resin concentrate, which still contains an appreciable proportion of coal (up to 15 to 20%) admixed therewith, is then dissolved in a solvent composed essentially of saturated hydrocarbons having 6 or less carbon atoms in accordance with the disclosure of the copending Lee application, Serial No. 515,804, filed December 27, 1943, now abandoned. The insoluble coal is separated from the resultin resin solution by filtration, and the resin itself is then recovered in a substantially coal-free'condition by vaporization of the solvent from the solution. If a light-colored resin product is desired, the resin solution may be filtered through a bed of activated clay or the like.
A typical Utah-type coal resin, recovered in this manner, is soluble in ethers, petroleum and coal-tar hydrocarbons, and vegetable oils, partially soluble in esters and ketones, and insoluble in the lower alcohols. The following physical and chemical characteristics are typical of a representative Utah-type coal resin which has been recovered by extraction with hexane:
Specific gravity 1.03-1.06 Softening point (mercury method)- C. Melting point (mercury method) 180 C.
Refractive index 1.544 Physical state Brittle solid Acid value 6-8 Iodine number 100-140 Molecular weight (average) 1000 Analysis:
Carbon 86.95% Hydrogen 11.10% Oxygen 1.95%
The coal resin is advantageously compounded with a butadiene-styrene rubbery copolymer, 'especially a copolymer containing from about 20% to about 30% styrene, in an amount ranging from about. 5 to about 25% based on the weightof the copolymer. Within this range of proportions occurs the most significant increase in processibility of the rubbery copolymer with the pro- 3 duction of a cured product having the most desirable characteristics. Less than 5% of the coal resin may be used, but in such case the increase in processibility of the copolymer may not be sufficient to permit the ready incorporation therewith of the desired amounts of pigments and fillers. More than 25% of the coal resin may also be employed. but in such event the cured compounded copolymer may be too boardy for certain applications. Suilicient coal resin should, of course, be incorporated with the butadiene-styrene copolymer to improve its processing characteristics and to enable it to be broken down on milling to the extent necessary for the desired purpose. The resin may be incorporated with the copolymer either before the copolymer is passed through a roll mill or other rubber handling equipment or during the milling of the copolymer.
The following examples illustrate typical formulations of GH rubber (a copolymer of about 75% butadiene and 25% styrene) compounded with a coal-free Utah-type coal resin:
Example 1 A GR-S-containing tire-tread stock was prepared from the following materials:
Parts by weight GR-S 250 Carbon .black 135 Utah-type coal resin (coal-free) 45 Zinc oxide Sulfur 6 Condensation product of mercaptobenzothiazole with cyclohexylamine 5 .25
The presence of the coal resin rendered the milling of the GR-S copolymer and the incorporation of the other ingredients therewith much more easy. The milled copolymer compound possessed an increased dry tack and exhibited an excellent tack when it was washed with gasoline.
Example 2 The following formulation illustrates a (33-8 copolymer compound having a very high degree of tackiness.
The compoundedGR-S was readily millable.
. g 4 The coal resin imparted an extremely high degree oi. tack to the copolymer compound as evidenced by the fact that two pieces of the milled compound were self-sealing when placed together. Samples of the milled compound were cured for one hour at 350 F. and were found to have the following properties:
Tensile strength --lbs. per sq. inch 1860 Elongation (ultimate) --per cent 2800 Shore hardness per cent We claim:
1. A composition comprising a rubbery copolymer of butadiene and styrene and 5-25% on the weight of the copolymer of a resin consisting essentially of carbon and hydrogen, having an average molecular weight on the order of 1000 and a refractive index of 1.544 and occurring in Utah resin-bearing coals.
2. The composition as claimed in claim 1, in which the rubbery copolymer of butadiene and styrene contains from about 20% to about 30% styrene.
3. The composition as claimed in claim 1, in which the rubbery copolymer of butadiene and styrene contains approximately butadiene and 25% styrene.
4. In the method of compounding a butadienestyrene rubbery copolymer, the steps of incorporating with such a copolymer 5 to 25%, based on the weight of the copolymer, of a resin consisting essentially of carbon and hydrogen, having an average molecular weight on the order of 1000 and a refractive index of 1.544 and occurring in Utah resin-bearing coals, and milling the mixture to obtain a rubber compound.
5. The method of compounding a butadienestyrene rubbery copolymer as claimed in claim 4 in which the rubbery copolymer contains from about 20% to about 30% styrene.
6. The method of compounding a butadienestyrene rubbery copolymer as claimed in claim 4 in which the rubbery copolymer contains approximately 75% butadiene and 25% styrene.
ERNEST D. LEE. LOY S. ENGLE.
REFERENCES CITED The following references are of record in the file of this patent:
UNITED STATES PATENTS Number Name Date 2,310,492 Nagelvoort Feb. 9, 1943 2,364,090 Nagelvoort Dec. 5, 1944 2,379,389 Tillotson June 26, 1945 2,382,731 Little Aug. 14, 1945
US640676A 1946-01-11 1946-01-11 Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal Expired - Lifetime US2461551A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US640676A US2461551A (en) 1946-01-11 1946-01-11 Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US640676A US2461551A (en) 1946-01-11 1946-01-11 Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal

Publications (1)

Publication Number Publication Date
US2461551A true US2461551A (en) 1949-02-15

Family

ID=24569250

Family Applications (1)

Application Number Title Priority Date Filing Date
US640676A Expired - Lifetime US2461551A (en) 1946-01-11 1946-01-11 Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal

Country Status (1)

Country Link
US (1) US2461551A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2582160A (en) * 1948-10-20 1952-01-08 Interchem Corp Butadiene-acrylonitrile copolymer composition containing a resin occuring in utah resin bearing coal
US2582139A (en) * 1949-07-08 1952-01-08 Interchem Corp Resinous products of the reaction of styrene with resins derived from bituminous coals of utah
US2673845A (en) * 1951-10-10 1954-03-30 Armstrong Cork Co Trowelable synthetic rubber adhesives

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2310492A (en) * 1940-12-05 1943-02-09 Nagelvoort Adriaan Recovering resins from coal
US2364090A (en) * 1942-02-23 1944-12-05 Nagelvoort Adrlaan Purifying resins
US2379389A (en) * 1942-12-14 1945-06-26 Neil E Tillotson Rubber or rubberlike composition and method
US2382731A (en) * 1942-09-26 1945-08-14 Hercules Powder Co Ltd Adhesive

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2310492A (en) * 1940-12-05 1943-02-09 Nagelvoort Adriaan Recovering resins from coal
US2364090A (en) * 1942-02-23 1944-12-05 Nagelvoort Adrlaan Purifying resins
US2382731A (en) * 1942-09-26 1945-08-14 Hercules Powder Co Ltd Adhesive
US2379389A (en) * 1942-12-14 1945-06-26 Neil E Tillotson Rubber or rubberlike composition and method

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2582160A (en) * 1948-10-20 1952-01-08 Interchem Corp Butadiene-acrylonitrile copolymer composition containing a resin occuring in utah resin bearing coal
US2582139A (en) * 1949-07-08 1952-01-08 Interchem Corp Resinous products of the reaction of styrene with resins derived from bituminous coals of utah
US2673845A (en) * 1951-10-10 1954-03-30 Armstrong Cork Co Trowelable synthetic rubber adhesives

Similar Documents

Publication Publication Date Title
EP0192930B1 (en) Natural rubber containing compositions with increased tear strength
US3519585A (en) Pressure sensitive adhesive composition
US3714110A (en) Oil extended polyurethanes based on hydroxy terminated diene polymers
US2638460A (en) Butadiene polymers as elastomer additives
JP3175016B2 (en) High hardness rubber composition
EP0020501A4 (en) Polymer compositions and a method for enhancement in phase compatibility of elastomers with relatively rigid polymers.
US2461551A (en) Composition comprising a rubbery copolymer of butadiene and styrene and a resin occurring in utah resinbearing coal
US2582264A (en) Softening agent for rubber and resulatant rubber composition
CA1128248A (en) Elastomers with improved metal adhesion
US2382731A (en) Adhesive
US2421627A (en) Rubberlike substances and compounding material
US2638456A (en) Plastic compound containing synthetic rubber and anthracite coal
US3238164A (en) Tall oil pitch-c1-c18 monohydric alcohol compositions and use thereof in rubber
US2440299A (en) Method of compounding rubbery materials
US2550363A (en) Lactam plasticizer for rubbers
US2582160A (en) Butadiene-acrylonitrile copolymer composition containing a resin occuring in utah resin bearing coal
US3243390A (en) Water-base paint containing hydrogenated hydrocarbon resin and butyl rubber
DE1073735B (en) Vulcanization of butyl rubber
US2537908A (en) Compounded rubber stock
US2461553A (en) Adhesive composition containing polychloroprene rubber and a resin occurring in utahresinbearing coal
US2427942A (en) Vulcanization of butadiene-styrene copolymer
US2340699A (en) Synthetic rubber composition
US2330698A (en) Plastic composition
US2794006A (en) Pan process of reclaiming rubber
US3231546A (en) Solid styrene-sulfur compounds and vulcanizates made therewith